<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>118(4)</volume><submitter>Jamois C</submitter><funding>Roche</funding><funding>F. Hoffmann-La Roche Ltd</funding><pubmed_abstract>The recent surge in T-cell-engaging and chimeric antigen receptor (CAR) T-cell therapies is changing the landscape of cancer therapy. Cytokine release syndrome (CRS) is a systemic inflammatory response syndrome that is a well-known complication of these therapies, of which interleukin-6 (IL-6) is a key mediator. Tocilizumab, an IL-6 receptor (IL-6R) antagonist, is approved for the management of CAR T-cell therapy-induced CRS in adults and in pediatric patients aged ≥ 2 years old. However, the approved dosing schedule was not based on IL-6R occupancy and may not be the most suitable schedule for T-cell-engaging therapies such as bispecific antibodies (bsAb) due to key differences in the levels of released IL-6, the clinical symptomatology of CRS, and the pharmacology of tocilizumab across s</pubmed_abstract><journal>Clinical pharmacology and therapeutics</journal><pagination>917-927</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12439009</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Tocilizumab Dosing for Management of T Cell-Engaging Bispecific Antibody-Related CRS in Patients With R/R B-Cell NHL.</pubmed_title><pmcid>PMC12439009</pmcid><pubmed_authors>Gibiansky L</pubmed_authors><pubmed_authors>Carlile DJ</pubmed_authors><pubmed_authors>Jamois C</pubmed_authors><pubmed_authors>Li F</pubmed_authors><pubmed_authors>Lundberg L</pubmed_authors><pubmed_authors>Frey N</pubmed_authors><pubmed_authors>Turner DC</pubmed_authors><pubmed_authors>Menuet JF</pubmed_authors><pubmed_authors>Kwan A</pubmed_authors><pubmed_authors>Wei MC</pubmed_authors><pubmed_authors>Guerini E</pubmed_authors><pubmed_authors>Grange S</pubmed_authors><pubmed_authors>Pereira LR</pubmed_authors><pubmed_authors>Relf J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Tocilizumab Dosing for Management of T Cell-Engaging Bispecific Antibody-Related CRS in Patients With R/R B-Cell NHL.</name><description>The recent surge in T-cell-engaging and chimeric antigen receptor (CAR) T-cell therapies is changing the landscape of cancer therapy. Cytokine release syndrome (CRS) is a systemic inflammatory response syndrome that is a well-known complication of these therapies, of which interleukin-6 (IL-6) is a key mediator. Tocilizumab, an IL-6 receptor (IL-6R) antagonist, is approved for the management of CAR T-cell therapy-induced CRS in adults and in pediatric patients aged ≥ 2 years old. However, the approved dosing schedule was not based on IL-6R occupancy and may not be the most suitable schedule for T-cell-engaging therapies such as bispecific antibodies (bsAb) due to key differences in the levels of released IL-6, the clinical symptomatology of CRS, and the pharmacology of tocilizumab across s</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Oct</publication><modification>2026-06-01T14:05:15.86Z</modification><creation>2026-04-08T13:20:41.031Z</creation></dates><accession>S-EPMC12439009</accession><cross_references><pubmed>40576759</pubmed><doi>10.1002/cpt.3751</doi></cross_references></HashMap>